Leukocyte traffic control: a novel therapeutic strategy for inflammatory bowel disease - an update

被引:1
|
作者
Cesarini, Monica [1 ]
Fiorino, Gionata [2 ]
机构
[1] Policlin Umberto 1, Dept Internal Med & Clin Sci, Rome, Italy
[2] Ist Ricovero & Cura Carattere Sci Humanitas, Inflammatory Bowel Dis Ctr, Milan, Italy
关键词
antiadhesion molecules; anti-integrins; Crohn's disease; inflammatory bowel disease; leukocyte recruitment; ulcerative colitis; vedolizumab; RECEPTOR ANTAGONIST CCX282-B; ACTIVE CROHNS-DISEASE; TRAFICET-EN; ULCERATIVE-COLITIS; DOUBLE-BLIND; INTEGRIN INHIBITOR; NATALIZUMAB; PROTECT-1; VEDOLIZUMAB; EFFICACY;
D O I
10.1586/ECI.13.11
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Adhesion molecules play a key role in the pathogenetic mechanisms of inflammatory bowel disease (IBD), both in Crohn's disease (CD) and ulcerative colitis (UC). In the last decade, some progress has been made in understanding their key role in leukocyte trafficking control in terms of basic research, but evidence of clinical efficacy is lacking. In the last 2 years, new molecules directed against integrins and integrin receptors have been developed and investigated in clinical trials, showing that anti-alpha 4 beta 7 integrin agents can be effective and safe for the induction and maintenance of remission in active CD and UC. Preliminary data show that anti-MAdCAM, anti-beta 7 and anti-integrin receptor agents are not all effective in IBD. Such results open new perspectives on clinical management of IBD, and new directions in understanding the role of adhesion molecules and leukocyte recruitment both in CD and UC.
引用
收藏
页码:301 / 306
页数:6
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